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European Journal of Human Genetics : EJHG|June 3, 1999
Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorderG R Verheyen, S M Villafuerte, J Del-Favero, et al.Journal of Human Hypertension|July 1, 1995
Lack of association between HLA class II polymorphisms and essential hypertension in a Belgian populationX X Gu, M Spaepen, P Raeymaekers, et al.Clinical Genetics|October 23, 1997
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, et al.American Journal of Medical Genetics|July 12, 1996
Linkage analysis in three families with nonspecific X-linked mental retardationS Claes, X X Gu, E Legius, et al.American Journal of Medical Genetics|September 12, 2000
Novel syndromic form of X-linked complicated spastic paraplegiaS Claes, K Devriendt, G Van Goethem, et al.Journal of the Neurological Sciences|May 1, 1992
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeV Timmerman, P Raeymaekers, E Nelis, et al.Neuropsychobiology|January 1, 1995
Manic-depressive illness and linkage reanalysis in the Xq27-Xq28 region of chromosome XK Mendelbaum, S Sevy, D Souery, et al.Journal of the Neurological Sciences|December 1, 1988
Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathyP Raeymaekers, P De Jonghe, L Swerts, et al.Cytogenetics and Cell Genetics|January 1, 1989
Exclusion analysis of Charcot-Marie-Tooth neuropathy (CMT1) with chromosome 1p markersP Raeymaekers, P De Jonghe, L Swerts, et al.FEBS Letters|September 25, 1989
DNA fingerprints revealing common and divergent human DNA methylation patternsZ N Berneman, P Raeymaekers, G Vanhoof, et al.Pageof 5